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  2. Chemical purity - Wikipedia

    en.wikipedia.org/wiki/Chemical_purity

    Reagent grade is almost as stringent as the ACS grade. USP grade meets the purity levels set by the United States Pharmacopeia (USP). USP grade is equivalent to the ACS grade for many drugs. NF grade is a purity grade set by the National Formulary (NF). NF grade is equivalent to the ACS grade for many drugs.

  3. United States Pharmacopeia - Wikipedia

    en.wikipedia.org/wiki/United_States_Pharmacopeia

    The USP is published in a combined volume with the National Formulary (a formulary) as the USP-NF. [2] If a drug ingredient or drug product has an applicable USP quality standard (in the form of a USP-NF monograph), it must conform in order to use the designation "USP" or "NF".

  4. Food Chemicals Codex - Wikipedia

    en.wikipedia.org/wiki/Food_Chemicals_Codex

    In response to these requests, advice was sought from special committees composed of representatives of industry, government agencies, and others experienced in the operation of the USP and the NF. [5] As a result, in 1966, This first edition of the FCC was published by the Institute of Medicine (IOM) for FDA. USP acquired the FCC in 2006.

  5. Tablet (pharmacy) - Wikipedia

    en.wikipedia.org/wiki/Tablet_(pharmacy)

    The simpler tests are often used for quality control purposes, whereas the more complex tests are used during the design of the formulation and manufacturing process in the research and development phase. Standards for tablet properties are published in the various international pharmacopeias (USP/NF, EP, JP, etc.).

  6. Emulsifying wax - Wikipedia

    en.wikipedia.org/wiki/Emulsifying_wax

    The ingredient name is often followed by the initials NF, indicating that it conforms to the specifications of the National Formulary. Emulsifying wax is created when a wax material (either a vegetable wax of some kind or a petroleum-based wax) is treated with a detergent (typically sodium dodecyl sulfate or polysorbates ) to cause it to make ...

  7. Dissolution testing - Wikipedia

    en.wikipedia.org/wiki/Dissolution_testing

    In United States Pharmacopeia (USP) General Chapter <711> Dissolution, there are four dissolution apparatuses standardized and specified. [6] They are: USP Dissolution Apparatus 1 – Basket (37 °C ± 0.5 °C ) USP Dissolution Apparatus 2 – Paddle (37 °C ± 0.5 °C) USP Dissolution Apparatus 3 – Reciprocating Cylinder (37 °C ± 0.5 °C)

  8. Suture materials comparison chart - Wikipedia

    en.wikipedia.org/wiki/Suture_materials...

    80% at 2 weeks, 44% at 8 weeks. Complete absorption within 200 days [2] Structure: Multifilament: Multifilament: Braided: Monofilament Origin: Bovine serosa surface finish. Made by twisting together strands of purified collagen taken from the small intestine of healthy ruminants: Bovine serosa. The natural chromic thread is precision ground in ...

  9. USP 800 - Wikipedia

    en.wikipedia.org/wiki/USP_800

    USP 800 (Hazardous Drugs—Handling in Healthcare Settings) is a guideline created by the United States Pharmacopeia Convention (USP), as one of their General Chapters through which the USP "sets quality standards for medicines, dietary supplements and food ingredients".